A supercapacitor electrode mechanism comprising an electrically conductive, porous substrate, having one or more metallic oxides deposited on a first surface and a chemically reduced graphene oxide deposited on a second surface, to thereby provide an electrical double layer associated with the substrate. The substrate may be carbon paper or a similar substance. The layers of the supercapacitor are optionally rolled into an approximately cylindrical structure.

Patent
   8940145
Priority
Mar 01 2013
Filed
Mar 01 2013
Issued
Jan 27 2015
Expiry
Mar 26 2033
Extension
25 days
Assg.orig
Entity
Large
14
7
EXPIRED<2yrs
1. A method for fabricating a supercapacitor, the method comprising:
providing an electrically conductive substrate, having spaced apart first and second surfaces;
providing a layer of metal oxides, including at least one of MnO2 and Co3O4, contiguous to the first substrate surface; and
providing a layer of chemically reduced graphene oxide (rGO) contiguous to the second substrate surface, to thereby provide an electrical double layer associated with the substrate.
2. The method of claim 1, further comprising providing, as said conductive substrate, a sheet of carbon paper comprising a cellulose substance impregnated with a combination of carbon nanotube ink and sodium dodecylbenzenesulfonate.
3. The method of claim 2, wherein said carbon paper has an associated capacitance of at least about 200 Farads/gm.
4. The method of claim 1, further comprising providing, as said conductive substrate, at least one of a layer of stainless steel, a thin metal foil and a semiconductor material with a dopant density of at least 1019 cm−3.
5. The method of claim 1, further comprising providing said rGO layer on said second substrate surface by a process comprising depositing a layer of graphene oxide on said second substrate surface, using electrophoretic deposition comprising providing at least one room temperature ionic liquid (RTIL) as an electrolyte for said rGO.
6. The method of claim 1, further comprising providing said rGO layer on said second substrate surface by a process comprising depositing a layer of graphene oxide on said second substrate surface, using electrophoretic deposition comprising at least one room temperature ionic liquid (RTIL) as an electrolyte and at least one solid polymer that manifests piezoelectrical behavior.
7. The method of claim 5, further comprising choosing said room temperature ionic liquid to comprise at least one of methyl imidazole, ammonium ions, 1-butyl-1-methylpyrrolldinium bis(trifluoromethylsulfonylimide, and methyltrioctylammonium bis(trifluoromethylsulfonyl)imide.
8. The method of claim 5, further comprising forming said electrical double layer at an interface between said reduced graphene oxide layer and said electrolyte.
9. The method of claim 1, further comprising providing said reduced graphene oxide using a substance comprising at least one of hydrazine and sodium borohydride as a reducing agent.
10. The method of claim 1, further comprising providing a distribution of said metal oxides in a first layer that serves as a first electrical terminal, providing said substrate in a second layer, providing a distribution of said chemically reduced graphene oxide in a third layer that serves as a second electrical terminal, and forming the first, second and third layers into a cylindrical structure.

The invention described herein was made in the performance of work under a NASA contract and by an employee of the United States Government and is subject to the provisions of Public Law 96-517 (35 U.S.C. §202) and may be manufactured and used by or for the Government for governmental purposes without the payment of any royalties thereon or therefore. In accordance with 35 U.S.C. §202, the contractor elected not to retain title.

This invention relates to nanofabrication of an electrode suitable for use in a supercapacitor.

A supercapacitor requires use of a substance that has a relatively high power density, which can be achieved with some materials, and simultaneously a relatively high energy density. Achievement of both of these conditions with a single material has not been possible in the prior art.

The invention meets these needs by providing a procedure for nanofabrication of an electrode mechanism, for use in a supercapacitor (SC) that has relatively high power density (100-200 KW/Kgm or higher) and simultaneously has relatively energy density (20 KW-hr/KGM or higher). The procedure includes the steps of: (1) providing a porous, electrically conductive substrate that has first and second, spaced apart surfaces; (2) depositing one or more selected metal oxides, including at least one of MnO2 and Co3O4, on the first substrate surface; and (3) depositing an assembly of chemically reduced graphene oxide (rGO) on the second substrate surface, to thereby provide an electrical double layer associated with the substrate.

FIG. 1 is a flow chart of a procedure for fabricating an electrode mechanism according to an embodiment of the invention.

FIG. 2 is a schematic view of a layered embodiment of the invention.

FIG. 3 illustrates a perspective end view of a cylindrical embodiment of the invention.

FIG. 1 is a flow chart of a procedure for fabricating an electrode mechanism according to an embodiment of the invention. In step 11, a porous, electrically conductive substrate is provided that has spaced apart, first and second, surfaces. The substrate can be a metal, such as stainless steel or thin metal foil, a doped semiconductor, such as Si doped at 1019 cm−3 or higher, carbon paper, such as Toray paper or Bucky paper, an electrically conducting polymer, or a cellulose substance (optionally including photocopy paper) impregnated with a combination of carbon nanotube (CNT) ink and sodium dodecylbenzesesulfonate, the carbon paper having a thickness in a range 500-2000 nm, or another conductive substance.

In step 12, one or more selected metal oxides, including at least one of MnO2 and Co3O4, is deposited on the first substrate surface. The metal oxide has an associated specific capacity of around 300 Farads/gm.

In a third step 13, an assembly of flakes or chips of reduced graphene oxide (rGO) is deposited on the second substrate surface, with individual flake thicknesses in a range 1-15 μm, depending upon the electrolyte. Deposition of the rGO can, for example, be achieved by deposit of graphene oxide (GO) on the substrate second surface, followed by electrophoretic deposition (EPD), such as cathodic deposition using an electrolyte such as a room temperature ionic liquid (RTIL).

An RTIL is a room temperature, liquid, solvent-free electrolyte. Examples of RTILs are 1-butyl-1-methylpyrrolldinium bis(trifluoromethylsulfonyl)imide, Methyltrioctylammonium bis(trifluoromethylsulfonyl)imide, ammonium ions, and methyl imidazole.

The reducing agent may be hydrazine, sodium borohydride, or a similar substance. The rGO helps provide an electrical double layer associated with the substrate.

FIG. 2 illustrates a three-layer, substantially planar embodiment 20t of the invention provided by the procedure discussed in FIG. 1, comprising a metallic oxide layer 21, a substrate 22 and an rGO layer 23, with associated electrical terminals 24 and 25. The electrolyte may be an RTIL or a combination of RTIL and a solid polymer (SP) that manifests at least some piezoelectric behavior.

This fabrication procedure also provides a three-layer (more generally, a multi-layer) cylindrical embodiment 30 in FIG. 3 for storage or transfer of an electrical charge with relatively high power density and energy density. The energy density and power density can be increased substantially by rolling this three-layer system into a 3N-layercylindrical system 30, as indicated in an end view in FIG. 3, with N>>1. In FIG. 3, the geometric structure is illustrated with N approximately equal to 2. The first layer 31 contains metallic oxides, the second layer 32 is a thicker substrate layer, and the third layer 33 includes rGO and a selected electrolyte. The substrate may have a thickness as small as 1-5 μm and as large as 150 μm depending upon the substrate material and the maximum permissible curvature of the geometric structure illustrated in FIG. 3. For a given substrate material, the smaller the substrate thickness, the greater the geometric structure that can be supported without substrate cracking or crazing. The layers illustrated in FIG. 3 are preferably rolled into a structure resembling a cylinder.

In an embodiment, illustrated in FIG. 2 or FIG. 3, the (solid or gel-like) electrolyte comprises a combination of an RTIL and a solid polymer SP, such as polyvinylidene fluoride or difluoride, preferably β-phase.

Ideally, the system should operate at temperatures in a range −40° C.<T<100° C., should operate at voltages in a range −3 to +7 Volts, and should rely upon non-toxic materials for fabrication. The system should be mechanically flexible and have a relatively small form factor.

It will be appreciated to those skilled in the art that the preceding examples and embodiment are exemplary and not limiting to the scope of the present invention. It is intended that all permutations, enhancements, equivalents, combinations, and improvements thereto that are apparent to those skilled in the art upon a reading of the specification and a study of the drawings are included within the true spirit and scope of the present invention.

Chen, Bin, Meyyappan, Meyya

Patent Priority Assignee Title
10067064, Jan 22 2013 Research & Business Foundation Sungkyunkwan University Optical fiber containing graphene oxide and reduced graphene oxide and a gas sensor containing the same
10340094, May 18 2015 Nokia Technologies Oy Apparatus and associated methods for electrical storage
11127941, Oct 25 2019 LYTEN, INC Carbon-based structures for incorporation into lithium (Li) ion battery electrodes
11127942, Oct 25 2019 LYTEN, INC Systems and methods of manufacture of carbon based structures incorporated into lithium ion and lithium sulfur (li s) battery electrodes
11133495, Oct 25 2019 LYTEN, INC Advanced lithium (LI) ion and lithium sulfur (LI S) batteries
11198611, Jul 30 2019 LYTEN, INC 3D self-assembled multi-modal carbon-based particle
11299397, Jul 30 2019 LYTEN, INC 3D self-assembled multi-modal carbon-based particles integrated into a continuous electrode film layer
11508966, Oct 25 2019 LYTEN, INC Protective carbon layer for lithium (Li) metal anodes
11539074, Oct 25 2019 LYTEN, INC Artificial solid electrolyte interface (A-SEI) cap layer including graphene layers with flexible wrinkle areas
11631893, Oct 25 2019 LYTEN, INC Artificial solid electrolyte interface cap layer for an anode in a Li S battery system
11735740, Oct 25 2019 Lyten, Inc. Protective carbon layer for lithium (Li) metal anodes
11735745, Jun 16 2021 LYTEN, INC Lithium-air battery
11870063, Oct 24 2022 Lyten, Inc. Dual layer gradient cathode electrode structure for reducing sulfide transfer
9997775, Aug 10 2016 The United States of America as represented by the Secretary of the Navy Reconfigurable liquid metal and graphene power source
Patent Priority Assignee Title
20120026643,
20130236785,
20130236786,
20140098461,
20140111906,
WO2010030361,
WO2011029006,
///
Executed onAssignorAssigneeConveyanceFrameReelDoc
Mar 01 2013The United States of America as Represented by the Administrator of the National Aeronautics & Space Administration (NASA)(assignment on the face of the patent)
Jun 11 2013LC TECHUSA AS REPRESENTED BY THE ADMINISTRATOR OF THE NASAASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0306270208 pdf
Jun 13 2013MEYYAPPAN, MEYYAUSA AS REPRESENTED BY THE ADMINISTRATOR OF THE NASAASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0306270258 pdf
Date Maintenance Fee Events
Jul 27 2018M1551: Payment of Maintenance Fee, 4th Year, Large Entity.
Sep 19 2022REM: Maintenance Fee Reminder Mailed.
Mar 06 2023EXP: Patent Expired for Failure to Pay Maintenance Fees.


Date Maintenance Schedule
Jan 27 20184 years fee payment window open
Jul 27 20186 months grace period start (w surcharge)
Jan 27 2019patent expiry (for year 4)
Jan 27 20212 years to revive unintentionally abandoned end. (for year 4)
Jan 27 20228 years fee payment window open
Jul 27 20226 months grace period start (w surcharge)
Jan 27 2023patent expiry (for year 8)
Jan 27 20252 years to revive unintentionally abandoned end. (for year 8)
Jan 27 202612 years fee payment window open
Jul 27 20266 months grace period start (w surcharge)
Jan 27 2027patent expiry (for year 12)
Jan 27 20292 years to revive unintentionally abandoned end. (for year 12)